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Poster Display session

458P - Treatability with combination chemotherapy and eligibility for addition of new drugs in all gastroesophageal cancer patients referred for medical treatment 2016-2022 at a tertiary centre serving 540.000 inhabitants

Date

27 Jun 2024

Session

Poster Display session

Presenters

Kaisa Lehtomaki

Citation

Annals of Oncology (2024) 35 (suppl_1): S162-S204. 10.1016/annonc/annonc1482

Authors

P.J. Osterlund, M.T. Barlund, A. Osterlund, J. Kontiainen, T. Mikkola, S. Kukkurainen, K.I. Lehtomaki

Author affiliations

  • Tampere University Hospital (Tays), Tampere/FI

Resources

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Abstract 458P

Background

Biological agents are increasingly added to combination chemotherapy (ComboCTx) in the care of gastroesophageal cancer (GEC), posing a challenge for patient selection. We investigated which real-world patients are treatable and eligible for ComboCTx.

Methods

We retrospectively analysed electronic health records for all GEC patients referred for medical treatment consideration at Tampere University Hospital (TUH) 2016-2022. Chi-square test and Kaplan-Meier estimates were used.

Results

During 7 years 577 patients were diagnosed with GEC in TUH district and 313 (54%) were referred for medical treatment consideration, and CTx given to 220 (70%). Demographics are presented in the table. ComboCTx was given to 84% and single agent (SingleCTx) in 16%. Treatment intent in ComboCTx and SingleCTx was curative in 53% and 29%, respectively, with median overall survival (mOS) 34 and 11 months, and palliative in 47% and 71% with mOS 10 and 11 months. Trastuzumab was added to palliative treatment in 13%. Other treatment without CTx, as surgery, chemoradiation or radiotherapy was given to 18%, mOS 43 months. Best supportive care only (BSC) was given to 12% with mOS 2 months. Ineligibility for new drugs (study inclusion/exclusion criteria not met) among CombCTx patients was 48% (90/186) due to ECOG PS >1 in 45, Charlson ≥4 in 9, non-adequate organ function in 36, second cancer within 5 years in 29, and not adenocarcinoma or squamous histology in 18 (histology missing in 74). Table: 458P

Patient characteristics

All ComboCTx SingleCTx Other BSC
313 (100%) 186 (59%) 34 (12%) 55 (18%) 36 (12%)
Curative treatment intent 48 % 53 % 28 % 73 % 0 %
Male sex 72 % 76 % 67 % 69 % 64 %
Age >75 years 27 % 15 % 58 % 44 % 31 %
Gastric primary 55 % 53 % 61 % 62 % 50 %
Primary not resected 57 % 50 % 75 % 40 % 100 %
Metastatic disease 38 % 35 % 44 % 22 % 72 %
Other cancers within 5 years 20 % 16 % 33 % 27 % 14 %
ECOG >1 44 % 24 % 81 % 24 % 97 %
Charlson ≥4 (n=310) 15 % 11 % 14 % 24 % 22 %
BMI<18.5 (n=282) 5 % 3 % 12 % 0 % 12 %
Non-adeno/SCC histology (n=238) 17 % 12 % 24 % 24 % 29 %
Non-adequate organ function (n=252) 36% 28 % 35 % 38% 66%

Conclusions

In our half million district more than half of all unselected patients diagnosed with GEC were considered for CTx and 70% of them received it. ComboCTx was given to 84% of CTx treated with survival in line with literature. Only half of the patients are eligible for addition of new biological drugs, if trial inclusion/exclusion criteria are used in the implementation.

Clinical trial identification

MJ006N, R19628S.

Legal entity responsible for the study

Tampere University Hospital.

Funding

Tampere University Hospital OOO project.

Disclosure

P.J. Osterlund: Financial Interests, Personal, Advisory Board, Also invited speaker: Amgen; Financial Interests, Personal, Advisory Board, Also invited speaker: AstraZeneca, MSD, BMS; Financial Interests, Personal, Advisory Board, Also invited lecturer: Bayer, Pierre Fabre; Financial Interests, Personal, Invited Speaker: Eisai, Fresenius Kabi, Imedex; Financial Interests, Personal, Advisory Board: Merck, Sanofi, Incyte, Daiichi Sankyo/AstraZeneca, Eisai, Jansen Pharmaceutica; Financial Interests, Personal, Invited Speaker, Roche Finland and Sweden: Roche; Financial Interests, Personal, Invited Speaker, No compensation for advisory boards: Servier; Financial Interests, Personal, Invited Speaker, Also via Medicom: Nordic Drugs/Group; Financial Interests, Personal, Expert Testimony, FIMEA expert testimony: BMS; Financial Interests, Personal, Invited Speaker, Nordic guidelines committee: Danone; Financial Interests, Institutional, Research Grant: Amgen, Servier, Nordic Drugs/Group; Financial Interests, Institutional, Invited Speaker: Incyte, Roche, Pfizer; Non-Financial Interests, Member: Colores patient advocacy group; Non-Financial Interests, Member, Board member: Finnish Cancer Society. J. Kontiainen: Financial Interests, Personal, Training, Travel costs: Novartis. K.I. Lehtomaki: Financial Interests, Institutional, Research Grant: Amgen, Merck, Roche, Sanofi, Servier, Eli Lilly; Financial Interests, Personal, Expert Testimony: Bayer, Amgen; Financial Interests, Personal, Expert Testimony, Invited speaker: Roche; Financial Interests, Personal, Invited Speaker: Servier, Pfizer, AstraZeneca. All other authors have declared no conflicts of interest.

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